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Ablation of Focal Activation in Atrial Fibrillation

Key facts

Where
London, United KingdomSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 85 years old?

Source: NCT06402617, who can take part

Where in United Kingdom

  • Hammersmith HospitalLondon, United KingdomTaking people

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  2. Are travel costs paid?
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  4. What happens if I want to stop?
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Trial details

Who runs it
Imperial College London
Trial code
NCT06402617
Record updated
9 November 2026
Original description
Recurrent focal electrical activation (or ectopy) superseding sinus activation is the only mechanism proven to drive paroxysmal atrial fibrillation (AF). However, it has not been possible to show similar focal drivers during AF, owing to the limitations of mapping in persistent AF. RETRO-Mapping has been developed as a method to generate activation maps during AF to test the hypothesis that persistent AF is also maintained by focal drivers.Read full original descriptionShow less

Ablation of Focal Activation During Persistent Atrial Fibrillation to Determine the Characteristics of Focal Drivers

Recurrent focal electrical activation (or ectopy) superseding sinus activation is the only mechanism proven to drive paroxysmal atrial fibrillation (AF). However, it has not been possible to show similar focal drivers during AF, owing to the limitations of mapping in persistent AF. RETRO-Mapping has been developed as a method to generate activation maps during AF to test the hypothesis that persistent AF is also maintained by focal drivers.

RETRO-Mapping is able to locate sites of focal activation that were isolated, intermittent, or recurrent during persistent AF. However, a 30-second segment of AF can have approximately 150 wavefronts in a small area of myocardium. Screening for focal activation and manually validating these prior to ablation was not feasible using current commercial systems.

RETRO-Mapping can automatically detect focal activation and a recording system that enables the intracardiac signals to be directly analysed by the RETRO-Mapping software. This will allow RETRO-Mapping to build a detailed classification of focal activation types and study the impact of ablation of these sites on the AF cycle length, to address the hypothesis that persistent AF is maintained by focal drivers.

Inclusion: Persistent atrial fibrillation with clinical indication for catheter ablation; Clinically suitable candidate for catheter ablation; Signed informed consent.

Exclusion: Previous atrial fibrillation or other catheter ablation procedure; Bleeding or clotting disorders, clinically high bleeding risk, or clinical contraindication to receiving heparin; Currently receiving or at risk of requiring renal replacement therapy; Clinical contraindication to catheter ablation or general anaesthetic, including history of adverse reaction to contrast media, or presence of intracardiac thrombus, or inadequate anticoagulation in the preceding 6 weeks; Valvular disease graded moderate or greater, or presence of a prosthetic valve; Active infection or fever; Severe cerebrovascular disease; Active gastrointestinal bleeding; Malignancy necessitating therapy; Moderate-to-severe heart failure, defined as left ventricular ejection fraction <35% and/or New York Heart Association class III-IV; Baseline serum creatinine >200umol/L; Uncontrolled diabetes (HbA1c ≥73mmol/mol or HbA1c ≤64mmol/mol and fasting blood glucose ≥9.2mmol/L); Any form of cardiomyopathy; Life expectancy shorter than the duration of the trial; Pregnancy, or childbearing potential and not using a highly effective method of contraception; Inability to provide informed consent to participate in the trial.

ClinicalTrials.gov NCT06402617